ZMP
ldlrap1b
Ensembl ID:
ZFIN ID:
Description:
low density lipoprotein receptor adapter protein 1 [Source:RefSeq peptide;Acc:NP_001074104]
Human Orthologue:
LDLRAP1
Human Description:
low density lipoprotein receptor adaptor protein 1 [Source:HGNC Symbol;Acc:18640]
Mouse Orthologue:
Ldlrap1
Mouse Description:
low density lipoprotein receptor adaptor protein 1 Gene [Source:MGI Symbol;Acc:MGI:2140175]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35584 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31964 | Essential Splice Site | Available for shipment | Available now |
| sa38970 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35584
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058093 | Nonsense | 43 | 229 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 46238863)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 45491827 |
| GRCz11 | 13 | 45612213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGGTGGAGGAACCCAAAGGAGAAGAGCTTTCAGCCGCTGCCGTCAAG[A/T]GAATCGTCGCTACTGTAAGACTCTGTACAGCAGCTCATCACACTGCACCC
Long Flanking Sequence:
ATATAATATAATAAACACACAAAGATCACAATGCAGAGATCTCTAAAGTCACAAAATAGCCTATGAGCTGTGAGAAATGTGACCTGAAGATTTTGAGAGATTCACCATCTGTAGTCTGTGTTGCCATGTTTTGGGTCCTGCTTGCATCATGTGTGCATGCTAATCCTGTGTGTGTGTGTGTGTGTGCATGTGAATGGAAGTATGGTCTTCATAAATATTAATGCATAATAATAATATAAATTGCACTTTTTCCATTACTAAAATGCTGCATATAGAATCAAAATGAAAACAACATGGCATACAAAGAAGAAAATATGTTAGTGGAAATCTGAAGTTCCATTAAATTAACTGTCTGTGTGTGTGTTTGTGTAGAGCTGCCGGAGAACTGGACGGACACACGGGAGACGCTATTGGAGGGGATGGTGTTTCAGCTGAAGTATCTGGGCATGACGCTGGTGGAGGAACCCAAAGGAGAAGAGCTTTCAGCCGCTGCCGTCAAG[A/T]GAATCGTCGCTACTGTAAGACTCTGTACAGCAGCTCATCACACTGCACCCAGAGACACTATTATTACTCTCAAACTGCCTGGAAAATTCACAAACACTTACAAAGAAAAAAAGAGAGAAAAGGGAAGAACTGTTAAATCACTCATGACTGTAGAAAAGTAGGTAAAAGATCAAGTGCACTTAACATTCAGTGACATTATTGAGGAAACACTTGTGCTTCTGTTTCTCTCAACTGTTTCATTATTTATTATTTATTTAAATCAATAGCATATTTAAAATATACATTTTCTTATTCTTCTTTTCTTTTAGCTTTCTTTCGTTCGTTCGTTCGTTCGTTTGTTTGTTTGTTCAGTCTGTCTGTCTGTAGTTCTATCATTCTATAGTTCTATCATCCCTCTCATCCATCCATCCATCCATTCACCCATCCATCCATCTATCCATCCACCCTTCGTTCAATCTATCCATCAGTCCATTGTTCTATTTATCCATCCATCCGTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31964
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058093 | Essential Splice Site | 47 | 229 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 46238847)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 45491811 |
| GRCz11 | 13 | 45612229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGGAGAAGAGCTTTCAGCCGCTGCCGTCAAGAGAATCGTCGCTACTG[T/A]AAGACTCTGTACAGCAGCTCATCACACTGCACCCAGAGACACTATTATTA
Long Flanking Sequence:
ACACAAAGATCACAATGCAGAGATCTCTAAAGTCACAAAATAGCCTATGAGCTGTGAGAAATGTGACCTGAAGATTTTGAGAGATTCACCATCTGTAGTCTGTGTTGCCATGTTTTGGGTCCTGCTTGCATCATGTGTGCATGCTAATCCTGTGTGTGTGTGTGTGTGTGCATGTGAATGGAAGTATGGTCTTCATAAATATTAATGCATAATAATAATATAAATTGCACTTTTTCCATTACTAAAATGCTGCATATAGAATCAAAATGAAAACAACATGGCATACAAAGAAGAAAATATGTTAGTGGAAATCTGAAGTTCCATTAAATTAACTGTCTGTGTGTGTGTTTGTGTAGAGCTGCCGGAGAACTGGACGGACACACGGGAGACGCTATTGGAGGGGATGGTGTTTCAGCTGAAGTATCTGGGCATGACGCTGGTGGAGGAACCCAAAGGAGAAGAGCTTTCAGCCGCTGCCGTCAAGAGAATCGTCGCTACTG[T/A]AAGACTCTGTACAGCAGCTCATCACACTGCACCCAGAGACACTATTATTACTCTCAAACTGCCTGGAAAATTCACAAACACTTACAAAGAAAAAAAGAGAGAAAAGGGAAGAACTGTTAAATCACTCATGACTGTAGAAAAGTAGGTAAAAGATCAAGTGCACTTAACATTCAGTGACATTATTGAGGAAACACTTGTGCTTCTGTTTCTCTCAACTGTTTCATTATTTATTATTTATTTAAATCAATAGCATATTTAAAATATACATTTTCTTATTCTTCTTTTCTTTTAGCTTTCTTTCGTTCGTTCGTTCGTTCGTTTGTTTGTTTGTTCAGTCTGTCTGTCTGTAGTTCTATCATTCTATAGTTCTATCATCCCTCTCATCCATCCATCCATCCATTCACCCATCCATCCATCTATCCATCCACCCTTCGTTCAATCTATCCATCAGTCCATTGTTCTATTTATCCATCCATCCGTCTGTTCATCCGTCCATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38970
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058093 | Essential Splice Site | 178 | 229 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 46220985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 45473949 |
| GRCz11 | 13 | 45630091 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCAGCTCTCAGTCCGAGAGTTCAGCCAGTCTGAGCAGCATGAAAGGAG[G/A]TGAACACACACACACACACACACACACACACACTCACACACATACCTGTA
Long Flanking Sequence:
TGTTTTATTTATAGTTTTAATGTTCATTCTTTCTATTGTTCATTCCATCACTATCTGTCATTTATTCTAACATTCTATCTATCGTTTTTTCTATCATTCTAGCTATCGTTCATTCTATTGTTCTATTGTCCTATCTGTTGTTCTATCTATCGCTTGTTCATCAGTCTATCTATTTATCTTTTGTTCCATCTATAATTCTTATATTCATTATATCTATTTTCATTCCATCACTCTGTCATTTATTCTATCATTCGTTCATACGGTTGATGTATTGTCCTATCTGTTGTTTTATCTATCTATTTTTCTATATATTGTTCTATCTATCACTCAGATGAAGAACTTGTTGACTGAATGCTTTATGTCACTGCACCATTCTCATGTTTCTGCTTTTACACTCTTGTTTTCAGAGAAAGAGAAGCAGGTGAAATGTGGCTCAGATGGAGAGGCAGCCAGCAGCTCTCAGTCCGAGAGTTCAGCCAGTCTGAGCAGCATGAAAGGAG[G/A]TGAACACACACACACACACACACACACACACACTCACACACATACCTGTACACGCATACACACATACATCACATGCAGCAGCACAACTTTAGCATTGTTGAAATCAAAATATGTTGCTAAAGCAAATGATCATGAGACACTGAAGCCCGGGGTGATGATGCTGACAATTCAGTTTTGAATCACAGGAATAAATTACATGTTTTCATTTCACAACACGCCAACATCATCTTGACTGAGCTGTCCAGAGAGGGTGTGGATGATAATACCAGGGCATTCTGAAAAAAAAAAGATCCTTCCAGTGGTAATACTAGTAGACCCAGGGATGATCATCTGACACCATCACTGAGCCATGGTGCTTTTTTTGTTAGAGTGCCAAAGGACCCTGAATGCTTCTCAGTTTGCCAGGTTACAGAAATAATCTTAGATGACAGAGTCGAGTGAACGAATGAACCCTTGAGGACCAGCCATCCGTGTGCTAGAGACAGACACGTGTGTATGTG
Associated Phenotype:
Not determined